US6114421A - Flame-retarding composition for polymers, preparation process and self-extinguishing polymeric products obtained therewith - Google Patents
Flame-retarding composition for polymers, preparation process and self-extinguishing polymeric products obtained therewith Download PDFInfo
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- US6114421A US6114421A US09/109,843 US10984398A US6114421A US 6114421 A US6114421 A US 6114421A US 10984398 A US10984398 A US 10984398A US 6114421 A US6114421 A US 6114421A
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- United States
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- flame
- self
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- Expired - Fee Related
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- 239000000203 mixture Substances 0.000 title claims abstract description 68
- 229920000642 polymer Polymers 0.000 title claims abstract description 46
- 238000002360 preparation method Methods 0.000 title claims abstract description 8
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims abstract description 44
- 229920000877 Melamine resin Polymers 0.000 claims abstract description 24
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 22
- 230000008569 process Effects 0.000 claims abstract description 21
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 18
- 238000006243 chemical reaction Methods 0.000 claims abstract description 16
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims abstract description 14
- 239000010452 phosphate Substances 0.000 claims abstract description 14
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000002253 acid Substances 0.000 claims abstract description 13
- 235000011180 diphosphates Nutrition 0.000 claims abstract description 13
- 239000002904 solvent Substances 0.000 claims abstract description 11
- 229920001577 copolymer Polymers 0.000 claims abstract description 9
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 claims abstract description 8
- 235000021317 phosphate Nutrition 0.000 claims description 15
- 239000000126 substance Substances 0.000 claims description 11
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 8
- 239000004952 Polyamide Substances 0.000 claims description 5
- 229920002647 polyamide Polymers 0.000 claims description 5
- 239000004793 Polystyrene Substances 0.000 claims description 4
- 239000003822 epoxy resin Substances 0.000 claims description 4
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 4
- 229920000647 polyepoxide Polymers 0.000 claims description 4
- 229920001225 polyester resin Polymers 0.000 claims description 4
- 239000004645 polyester resin Substances 0.000 claims description 4
- 229920000098 polyolefin Polymers 0.000 claims description 4
- 229920002223 polystyrene Polymers 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000001488 sodium phosphate Substances 0.000 claims description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 4
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 2
- 238000002425 crystallisation Methods 0.000 claims description 2
- 238000004821 distillation Methods 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- 230000035484 reaction time Effects 0.000 claims description 2
- 229910000162 sodium phosphate Inorganic materials 0.000 claims description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 1
- 230000008025 crystallization Effects 0.000 claims 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 claims 1
- 229920000058 polyacrylate Polymers 0.000 claims 1
- 239000002270 dispersing agent Substances 0.000 abstract description 7
- 239000000725 suspension Substances 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- 239000003795 chemical substances by application Substances 0.000 description 5
- -1 etc. Polymers 0.000 description 5
- 239000004114 Ammonium polyphosphate Substances 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 4
- 229920001276 ammonium polyphosphate Polymers 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 230000004075 alteration Effects 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 239000007857 degradation product Substances 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000011256 inorganic filler Substances 0.000 description 2
- 229910003475 inorganic filler Inorganic materials 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000003801 milling Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical class OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- 229920001187 thermosetting polymer Polymers 0.000 description 2
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 2
- 235000019801 trisodium phosphate Nutrition 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004594 Masterbatch (MB) Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000006253 efflorescence Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- YAMHXTCMCPHKLN-UHFFFAOYSA-N imidazolidin-2-one Chemical compound O=C1NCCN1 YAMHXTCMCPHKLN-UHFFFAOYSA-N 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- NQQWFVUVBGSGQN-UHFFFAOYSA-N phosphoric acid;piperazine Chemical class OP(O)(O)=O.C1CNCCN1 NQQWFVUVBGSGQN-UHFFFAOYSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000011008 sodium phosphates Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
- C09K21/06—Organic materials
- C09K21/12—Organic materials containing phosphorus
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3442—Heterocyclic compounds having nitrogen in the ring having two nitrogen atoms in the ring
- C08K5/3462—Six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34922—Melamine; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/34—Heterocyclic compounds having nitrogen in the ring
- C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
- C08K5/3477—Six-membered rings
- C08K5/3492—Triazines
- C08K5/34928—Salts
Definitions
- the present invention relates to a flame-retarding composition for polymers, copolymers and mixtures thereof, such as polyolefins, polyamides, etc., as well as epoxy resins, polyester resins, and the like.
- the invention also relates to a process for the preparation of said composition, as well as the polymers, copolymers, mixtures thereof, thermoplastic and thermosetting resins, and various polymeric materials such as paints, fabrics and the like, which are rendered self-extinguishing by means of said flame-retarding composition.
- a polymeric material is generally caused to become “self-extinguishing” or "anti-flame” or “flame-resistant” by the addition of particular "anti-flame” or “flame-retarding” agents, that can just impart the polymer substance the self-extinguishing characteristics required.
- anti-flame agents are constituted by organic halogenated, usually brominated substances, metal compounds (in particular oxides, such as for instance antimony trioxide), phosphorus and derivatives thereof (such as for instance red phosphorus, ammonium polyphosphate, organic phosphoric esters), various nitrogen-containing compounds (such as for instance urea, dicyandiamide, melamine), and still other ones.
- the formulations of polymer articles having self-extinguishing and intumescent characteristics comprise the polymer and at least two basic additives: a phosphorus-containing one, and a nitrogen- and/or nitrogen/carbon-containing one.
- a typical example is ammonium polyphosphate which, utilised in the right concentration, imparts the polymer composition class U L 94 VO self-extinguishing characteristics.
- the effectiveness of the product as concerns the self-extinguishing capacity is markedly improved by the addition of synergistic components containing nitrogen and/or phosphorus (melamine, melamine phosphates and pyrophosphates, ammonium polyphosphate, products of ethylenurea and formaldehyde condensation) and minor additives (silica, silicic acid, and titanium dioxide).
- synergistic components containing nitrogen and/or phosphorus melamine, melamine phosphates and pyrophosphates, ammonium polyphosphate, products of ethylenurea and formaldehyde condensation
- minor additives silica, silicic acid, and titanium dioxide.
- the so formulated preparations perform well as concerns self-extinguishing capacity (UL 94; total combustion time; oxygen index).
- Object of the invention is to realize and provide an anti-flame or flame-retarding composition for polymeric substances, suitable to impart the self-extinguishing polymer obtained excellent characteristics of self-extinguishing and intumescence, and ensuring also to the same polymer excellent characteristics of thermal stability and water resistance.
- a further object of the invention is to provide a flame-retarding composition for polymeric substances comprising several active anti-flame constituents associated into a single component or product perfectly homogeneous and such as to ensure a high use effectiveness.
- Still a further object of the invention is to provide a process for the preparation of said flame-retarding composition for polymeric materials suitable to ensure a perfect homogeneity to said composition.
- Still a further object of the invention is to provide a process allowing to obtain said flame-retarding composition substantially free from degradation substances and/or undesired by-products and with very high yields, substantially of 100%.
- a flame-retarding or anti-flame composition for polymers, copolymers, mixed polymers and mixtures thereof which composition according to the present invention comprises piperazine diacid pyrophosphate, piperazine acid phosphate, melamine acid phosphate and melamine.
- said flame-retarding composition comprises:
- composition according to the invention may also comprise one or more alkaline phosphates and/or pyrophosphates, in an amount of 5 to 15% by weight based on the total weight of the composition.
- the flame-retarding composition according to the present invention is advantageously used in particular to render polyolefins, polyamides, epoxy resins, polyester resins, polystyrene, acrylic, acrylic/styrenic polymers and the like self-extinguishing.
- the flame-retarding composition according to the present invention is substantially pure, more particularly it is free from products deriving from the alteration and/or polymerisation of the various constituents and/or the raw materials used for the preparation of said composition. Besides, the composition is perfectly and intimately homogeneous.
- composition according to the invention is used as a single component to be added to the above polymeric substances to render them self-extinguishing.
- composition according to the invention exercises its anti-flame activity without giving rise to substantial alterations of the chemical-physical and/or mechanical characteristics of the polymer wherein it is incorporated, and without causing solubilisation, migration, extraction or like phenomena.
- the composition according to the present invention allows to reach the desired levels of self-extinguishing of the polymers wherein it is incorporated, without needing to have recourse to the association with other products, such as for instance urea, dicyandiamide, melamine and/or salts thereof, such as for instance cyanurated melamine, whose use, as is known, involves remarkable and severe drawbacks because of the chemical, physical and mechanical characteristics of the self-extinguishing-rendered polymeric material.
- other products such as for instance urea, dicyandiamide, melamine and/or salts thereof, such as for instance cyanurated melamine
- the flame-retarding composition according to the present invention is of general use and may be advantageously employed for polymers, copolymers and polyolefinic mixed polymers (such as polyethylene, polypropylene, ethylene-propylene rubbers, etc.), for styrenic polymers (such as polystyrene, shockproof polystyrene, ABS, SBS resins, and the like), for polyurethanes, thermosetting resins such as unsaturated epoxy and polyester resins.
- the composition according to the present invention may also be used to render various polymer-based materials self-extinguishing, such as for instance paints, fabrics, carpet sizes, glues, latices and the like.
- an amount of composition of 10 to 45% by weight based on the weight of the self-extinguishing-rendered polymer is incorporated in the polymer or polymeric material.
- the incorporated composition amount is 15 to 35% by weight based on the weight of the self-extinguishing-rendered polymer.
- composition added in the amount of 20-45 parts per every 100 parts of polypropylene generates an intumescent article having excellent self-extinguishing properties.
- the flame-retarding composition according to the present invention allows the simultaneous use in the self-extinguishing-rendered polymer of stabilising-antioxidant agents of a known type, lubricants, dyes, inorganic fillers, mineral fibres and the like.
- constituents of the anti-flame composition according to the present invention are incorporated in the polymers according to known techniques, that vary each time according to the polymer.
- the incorporation may take place by blending-melting at the plastic state in screw extruders.
- the same composition in order to facilitate the dosage (absence of powders) and the dispersion of the flame-retarding composition in the polymeric materials to be rendered self-extinguishing, the same composition may be compounded and granulated with an amount of 10-30% of a wax or a polymeric substance compatible with the polymer wherein it has to be incorporated, with functions of binding-vehiculating means of the flame-retarding composition, as well as with other possible conventional additives, such as adjuvants, dyes, lubricants, antistatic agents, inorganic fillers, and the like.
- the process for the preparation of the aforesaid flame-retarding composition for polymers, copolymers, mixed polymers and mixtures thereof comprising piperazine diacid pyrophosphate, piperazine acid phosphate, melamine acid phosphate, melamine and possibly alkaline phosphates and/or pyrophosphates consists in reacting with water a mixture comprising phosphoric anhydride, piperazine and melamine intimately mixed with each other in the desired stoichiometric amounts and in suitably controlled time and temperature conditions.
- said water is added to the mixture comprising phosphoric anhydride, piperazine and melamine in form of crystallisation water of a suitable hydrated salt, such as for instance dodecahydrated sodium phosphate.
- the so obtained flame-retarding composition shows a perfect homogeneity and an ensuing constant chemical composition extended to the whole mass.
- the reaction temperature is preferably kept between about 50 and 100° C., in particular, in the starting stage, at 60-70° C.
- the conversion yields are very high, up to and over 99%, which causes the process to be very convenient from an economic point of view, and also ensures that the obtained composition is substantially free from degradation products and by-products.
- the reaction water is added in the form of a mixture with a suitable solvent/dispersant, which is thereafter separated from the composition and recovered at the end of the reaction by known filtration, distillation and like processes.
- said solvent/dispersant liquid medium has a function of solvent for one or more of the reacting species, of dispersant for the reaction mass, of thinner, and allows therefore to control the reaction progress by suitably adjusting the water/solvent medium ratio, besides subtracting excess heat during the reaction, exploiting also the evaporation heat of the same solvent.
- Said solvent/dispersant medium is advantageously selected from among dioxane, tetrahydrofuran, dimethyl sulfoxide, diethers and the like.
- the process yields are very high, up to and over 99%.
- the mass is stirred and, under constant cooling, a solution is fed comprising 90 g water and 300 g tetrahydrofuran in a period of time of 2-4 hours, keeping the temperature under 60° C.
- the mass is transferred to a drying chamber in order to evaporate the dispersant (solvent).
- the so obtained product undergoes a subsequent milling or screening to obtain the particle size desired ( ⁇ 100 ⁇ m).
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Fireproofing Substances (AREA)
Abstract
Description
______________________________________
Piperazine diacid pyrophosphate
45 to 65% by weight
Piperazine acid phosphate 2.5 to 4% by weight
Melamine acid phosphate 5 to 10% by weight
Melamine 15 to 30% by weight
______________________________________
______________________________________ melamine 300 g piperazine 200 g phosphoric anhydride 340 g ______________________________________
______________________________________ tetrahydrofuran 700 g melamine 300 g piperazine 200 g phosphoric anhydride 340 g anhydrous trisodium phosphate 70 g ______________________________________
Claims (11)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT97MI001805A IT1293495B1 (en) | 1997-07-29 | 1997-07-29 | FLAME RETARDANT COMPOSITION FOR POLYMERS, PREPARATION PROCESS AND OBTAINED SELF-EXTINGUISHING POLYMER PRODUCTS |
| ITMI97A1805 | 1997-07-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US6114421A true US6114421A (en) | 2000-09-05 |
Family
ID=11377657
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/109,843 Expired - Fee Related US6114421A (en) | 1997-07-29 | 1998-07-02 | Flame-retarding composition for polymers, preparation process and self-extinguishing polymeric products obtained therewith |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US6114421A (en) |
| EP (1) | EP0894820B1 (en) |
| AT (1) | ATE407174T1 (en) |
| DE (1) | DE69839955D1 (en) |
| ES (1) | ES2313740T3 (en) |
| IT (1) | IT1293495B1 (en) |
Cited By (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002002184A1 (en) | 2000-06-30 | 2002-01-10 | Medtronic, Inc. | Implantable medical device having flat electrolytic capacitor with tailored anode layers |
| DE10145093A1 (en) * | 2001-09-13 | 2003-04-10 | Chem Fab Budenheim Kg | Process for the preparation of polyphosphates of organic bases |
| US20030129902A1 (en) * | 2001-11-15 | 2003-07-10 | Hensler Connie D. | Textile products having flame retardant properties and methods of manufacture |
| US20040138351A1 (en) * | 2002-11-04 | 2004-07-15 | Nikolas Kaprinidis | Flame retardant compositions |
| WO2004078878A1 (en) * | 2003-03-05 | 2004-09-16 | Maya Meltzer Kasowski | Reaction product of a phosphorous acid with ethyleneamines for flame resistance |
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| US20050285300A1 (en) * | 2003-10-17 | 2005-12-29 | George Hairston | Plastic articles of enhanced flame resistance and related method |
| US20050287894A1 (en) * | 2003-07-03 | 2005-12-29 | John Burns | Articles of enhanced flamability resistance |
| US20060030227A1 (en) * | 2004-08-06 | 2006-02-09 | George Hairston | Intumescent flame retardent compositions |
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| CN114181397A (en) * | 2021-12-16 | 2022-03-15 | 北京工商大学 | Multi-block or random copolymerization halogen-free flame-retardant macromolecule and flame-retardant polyolefin material thereof |
| CN118404668A (en) * | 2024-05-28 | 2024-07-30 | 南京林业大学 | A method for preparing bamboo-based composite coil |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102007039560A1 (en) | 2007-08-22 | 2009-02-26 | Clariant International Limited | Flame-resistant plastic molding compound |
| MX2013006823A (en) | 2010-12-17 | 2013-08-26 | Dow Global Technologies Llc | Halogen-free, flame retardant composition for wire and cable applications. |
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| WO2002002184A1 (en) | 2000-06-30 | 2002-01-10 | Medtronic, Inc. | Implantable medical device having flat electrolytic capacitor with tailored anode layers |
| US20040260089A1 (en) * | 2001-09-13 | 2004-12-23 | Thomas Futterer | Method for producing polyphosphates of organic bases |
| US20080081856A1 (en) * | 2001-09-13 | 2008-04-03 | Karl Gotzmann | Process for the preparation of polyphosphates of organic bases |
| WO2003024945A3 (en) * | 2001-09-13 | 2003-08-14 | Budenheim Rud A Oetker Chemie | Method for producing polyphosphates of organic bases |
| US7345168B2 (en) * | 2001-09-13 | 2008-03-18 | Chemische Fabrik Budenheim Kg | Process for the preparation of polyphosphates of organic bases |
| US7893142B2 (en) | 2001-09-13 | 2011-02-22 | Chemische Fabrik Budenheim Kg | Process for the preparation of polyphosphates of organic bases |
| KR100897394B1 (en) * | 2001-09-13 | 2009-05-14 | 케미쉐 파브릭 부덴하임 카게 | Process for preparing polyphosphate of organic base |
| RU2322441C2 (en) * | 2001-09-13 | 2008-04-20 | Хемише Фабрик Буденхайм Кг | Method of preparing polyphosphates of organic compounds |
| DE10145093A1 (en) * | 2001-09-13 | 2003-04-10 | Chem Fab Budenheim Kg | Process for the preparation of polyphosphates of organic bases |
| US7455898B2 (en) * | 2001-11-15 | 2008-11-25 | Interface, Inc. | Textile products having flame retardant properties and methods of manufacture |
| US20030129902A1 (en) * | 2001-11-15 | 2003-07-10 | Hensler Connie D. | Textile products having flame retardant properties and methods of manufacture |
| US7736716B2 (en) | 2001-11-15 | 2010-06-15 | Interface, Inc. | Textile products having flame retardant properties and methods of manufacture |
| US7011724B2 (en) * | 2001-11-15 | 2006-03-14 | Interface, Inc. | Textile products having flame retardant properties and methods of manufacture |
| US20060121238A1 (en) * | 2001-11-15 | 2006-06-08 | Hensler Connie D | Textile products having flame retardant properties and methods of manufacture |
| US20090075017A1 (en) * | 2001-11-15 | 2009-03-19 | Interface, Inc. | Textile products having flame retardant properties and methods of manufacture |
| US7138448B2 (en) | 2002-11-04 | 2006-11-21 | Ciba Specialty Chemicals Corporation | Flame retardant compositions |
| US20040138351A1 (en) * | 2002-11-04 | 2004-07-15 | Nikolas Kaprinidis | Flame retardant compositions |
| US20060175587A1 (en) * | 2003-03-05 | 2006-08-10 | Kasowski Maya M | Reaction product of a phosphorous acid with ethyleneamines for flame resistance |
| WO2004078878A1 (en) * | 2003-03-05 | 2004-09-16 | Maya Meltzer Kasowski | Reaction product of a phosphorous acid with ethyleneamines for flame resistance |
| US20050054553A1 (en) * | 2003-06-27 | 2005-03-10 | The Procter & Gamble Company | Liquid fabric softening compositions comprising flame retardant |
| US20050287894A1 (en) * | 2003-07-03 | 2005-12-29 | John Burns | Articles of enhanced flamability resistance |
| US20050285300A1 (en) * | 2003-10-17 | 2005-12-29 | George Hairston | Plastic articles of enhanced flame resistance and related method |
| US20060030227A1 (en) * | 2004-08-06 | 2006-02-09 | George Hairston | Intumescent flame retardent compositions |
| US20060046591A1 (en) * | 2004-08-31 | 2006-03-02 | George Hairston | Mattress covers of enhanced flammability resistance |
| US8604105B2 (en) | 2010-09-03 | 2013-12-10 | Eastman Chemical Company | Flame retardant copolyester compositions |
| US8969443B2 (en) | 2010-09-03 | 2015-03-03 | Eastman Chemical Company | Flame retardant copolyester compositions |
| CN105837855A (en) * | 2016-05-10 | 2016-08-10 | 金发科技股份有限公司 | Halogen-free flame retardant and preparation method thereof and flame-retardant polyolefin composition composed of same |
| CN105837855B (en) * | 2016-05-10 | 2018-09-28 | 金发科技股份有限公司 | A kind of halogen-free flame retardants and preparation method thereof and the flame retardant polyolefin compound being made from it |
| CN110819009A (en) * | 2019-09-02 | 2020-02-21 | 上海化工研究院有限公司 | High-melt-index halogen-free flame-retardant polypropylene material and preparation method thereof |
| CN110819009B (en) * | 2019-09-02 | 2022-09-20 | 上海化工研究院有限公司 | High-melt-index halogen-free flame-retardant polypropylene material and preparation method thereof |
| CN114181397A (en) * | 2021-12-16 | 2022-03-15 | 北京工商大学 | Multi-block or random copolymerization halogen-free flame-retardant macromolecule and flame-retardant polyolefin material thereof |
| CN118404668A (en) * | 2024-05-28 | 2024-07-30 | 南京林业大学 | A method for preparing bamboo-based composite coil |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0894820A1 (en) | 1999-02-03 |
| ITMI971805A1 (en) | 1999-01-29 |
| DE69839955D1 (en) | 2008-10-16 |
| EP0894820B1 (en) | 2008-09-03 |
| IT1293495B1 (en) | 1999-03-01 |
| ES2313740T3 (en) | 2009-03-01 |
| ATE407174T1 (en) | 2008-09-15 |
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